Medical Writer (m/f/d)

At Optimapharm, you'll have the opportunity to work on diverse and meaningful projects that help bring innovative therapies to patients worldwide. As part of our international team, you'll collaborate with experts across multiple disciplines, gain exposure to a broad range of therapeutic areas, and contribute to research that makes a real difference.

With colleagues in 26 countries and operations in more than 40 countries, we combine global reach with the agility, collaboration, and supportive culture of a mid-sized organisation. Here, your expertise is valued, your growth is encouraged, and your work has a visible impact.

We are looking for a Medical Writer with proven experience in non-interventional studies (NIS), observational research, and Real-World Evidence (RWE) projects to join our Medical Affairs team. Working across both interventional and non-interventional research, you will play a key role in transforming complex clinical and real-world data into clear, scientifically robust deliverables that help our clients generate meaningful evidence and improve patient outcomes worldwide.

• Master's degree or higher in a medical, life science, pharmacy, epidemiology, or related field.
• At least 3 years of medical or scientific writing experience within a CRO, pharmaceutical, biotech, or medical device environment.
• Proven experience supporting non-interventional studies (NIS), observational research, patient registries, and/or Real-World Evidence (RWE) projects.
• Strong understanding of clinical research, regulatory requirements, and medical writing standards.
• Experience developing clinical, scientific, regulatory, and publication documents.
• Familiarity with FDA, EMA, ICH, and applicable observational research guidelines.
• Excellent communication, analytical, and literature review skills.

• →Author, review, and finalize clinical, scientific, regulatory, and publication documents.
• →Lead medical writing activities for interventional and non-interventional studies, including Real-World Evidence (RWE) and observational research projects.
• →Develop study protocols, study reports, manuscripts, abstracts, posters, and other scientific deliverables.
• →Collaborate with cross-functional teams to ensure scientific accuracy, consistency, and timely delivery of documents.
• →Manage document review cycles and incorporate stakeholder feedback effectively.
• →Ensure compliance with applicable regulations, guidelines, SOPs, and client requirements.
• →Conduct literature reviews and support the interpretation and communication of clinical and real-world data.
• →Contribute to process improvements, quality initiatives, and the development of internal documentation.
• →Stay up to date with evolving regulatory requirements, industry trends, and medical writing best practices.

If you would be interested in joining the Optimapharm team, please send your CV and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.

Compensation is competitive and final offers will reflect each candidate’s experience, skills, and qualifications.

Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required.